What it is
DSIP stands for delta sleep-inducing peptide. It is nine amino acids long, and it was first isolated in the 1970s from the cerebral venous blood of rabbits that had been put into a sleep-like state.
The name records the original observation: transferring the substance appeared to induce delta-wave sleep, the slow brain activity that characterises deep sleep. It is the oldest of the compounds sold for sleep. The wake system it would have to overcome runs largely on orexin (hypocretin), whose loss is associated with most human narcolepsy.
It is one of the oldest compounds in this library.
What the age tells you
That date is the most useful fact on this page.
DSIP has had roughly fifty years. It has a plausible mechanism, an obvious and enormous commercial target, and no regulatory obstacle standing in the way of anyone developing it. Sleep drugs are among the most valuable products in medicine.
And it has never been approved as a medicine anywhere.
Epitalon has a similar age and a similar shape of record. Compounds do not sit unexploited for half a century because nobody noticed. They sit that way because the effect proved hard to reproduce, or too small to matter, or too inconsistent to build on. No single paper announces this. It is visible only in the shape of the record.
What the human research shows
Small, old, and inconsistent. Some studies reported effects on sleep measures; others did not. The work never accumulated into anything larger.
This is a recognisable pattern: a striking original observation that becomes harder to see the more carefully it is looked for. It is not proof the effect is absent. It is what an effect that is absent, or very small, looks like from the outside.
The claims that came later
DSIP is also sold for stress resilience, pain and withdrawal symptoms. These rest on less than the sleep claim, which is already weak.
When a compound accumulates additional indications over decades while its original one remains unestablished, the additions are usually marketing rather than discovery.
What regulators have and have not said
For most of its fifty years DSIP was not prominent on regulators' lists, and that is easy to misread as a clean bill of health.
Regulators assess and restrict what someone is actively trying to compound or sell at scale. Being left alone reflected the absence of commercial pressure, not a finding about safety. Absence of a restriction was absence of attention.
That attention arrived once someone asked to compound it. FDA reviewed it on 24 July 2026 under its international name, emideltide, as a candidate for pharmacy compounding for insomnia and opioid withdrawal. Its briefing found no study of the injected route that was proposed, only intravenous data, and called the substance inadequately characterised. Unlike the six other peptides on that week's agenda, the committee agreed, voting 6 to 7 against (STAT, RAPS).
Last checked
2026-09-07.
